Abstract

Recoverin-antibody-related disease is currently restricted to late-onset ataxia and autoimmune retinopathy, which can be paraneoplastic or not. However, cognitive dysfunction associated with recoverin antibodies has not been reported so far in a homogeneous patient group. Our case series is dedicated to describing the novel phenotype of cognitive impairment associated with recoverin antibodies. We included five patients with cognitive impairment who presented serum recoverin autoantibodies detected by immunoblots in our case series investigation. We also analyzed their psychopathology, clinical data, cerebrospinal fluid (CSF), and neuroimaging data. Five patients with cognitive impairment associated with serum recoverin antibodies exhibited profound dysfunctional learning and verbal memory. In the CSF of 40% of them, we also diagnosed axonal neurodegeneration entailing elevated tau and phosphorylated tau protein levels. Psychopathologies such as affective symptoms (restlessness, depressive mood, anxiety, complaintiveness) and formal thought disorder, such as rumination, were detected in 25–75% of the patients. We hypothesized a role of recoverin autoimmunity in the pineal gland involving consecutive modulation of hippocampus-based memory caused by an altered release of melatonin. We describe a novel phenotype of possible recoverin autoimmunity in patients with cognitive impairment. However, no clear diagnostic clues can be extracted because of the low diagnostic validity of the testing strategies applied. The possibility of recoverin antibody autoimmunity in the pineal gland correlating with a modulation of hippocampus-based memory should be further investigated.

Highlights

  • Recoverin antibodies are known to be associated with both paraneoplastic and nonparaneoplastic retinopathy [1,2,3,4] and late-onset ataxia without retinopathy [5]

  • We describe a novel phenotype of possible recoverin autoimmunity in patients with cognitive impairment

  • The patients were screened for antibodies against ANNA-3, Ri, Hu, Yo, Tr/DNER, Ma/Ta, amphiphysin, aquaporin 4, myelin oligodendrocytic glycoprotein (MOG), N-methyl-D-asparate receptor (NMDAR), gamma amino butyric acid B receptor (GABABR), α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR), glycine receptor (GlyR), leucin glioma inactivated protein 1 (LGI1), contactinassociated protein-like 2 (CASPR2), IgLON5, recoverin, Zic4, dipeptidyl-peptidase-like protein 6 (DPPX) and myelin

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Summary

Introduction

Recoverin antibodies are known to be associated with both paraneoplastic and nonparaneoplastic retinopathy [1,2,3,4] and late-onset ataxia without retinopathy [5]. Cognitive dysfunction with recoverin antibodies has not yet been reported in patients. Recoverin is a calcium sensor protein in the nervous system located in the retina and pineal gland [6,7,8,9]. We report the novel phenotypic feature of cognitive dysfunction associated with recoverin antibodies

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